An Overview of Engineered Hydrogel-Based Biomaterials for Improved β-Cell Survival and Insulin Secretion

被引:20
作者
Ghasemi, Azin [1 ]
Akbari, Elham [1 ]
Imani, Rana [1 ]
机构
[1] Amirkabir Univ Technol, Dept Biomed Engn, Tehran Polytech, Tehran, Iran
来源
FRONTIERS IN BIOENGINEERING AND BIOTECHNOLOGY | 2021年 / 9卷
关键词
diabetes; hydrogels; insulin secretion; biomaterials; islet encapsulation; MESENCHYMAL STEM-CELLS; PANCREATIC-ISLET ENGRAFTMENT; ENDOTHELIAL GROWTH-FACTOR; TYPE-1; DIABETIC-PATIENT; EXTRACELLULAR-MATRIX; BIOARTIFICIAL PANCREAS; ALLOGRAFT-REJECTION; ALGINATE; TRANSPLANTATION; ENCAPSULATION;
D O I
10.3389/fbioe.2021.662084
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Islet transplantation provides a promising strategy in treating type 1 diabetes as an autoimmune disease, in which damaged beta-cells are replaced with new islets in a minimally invasive procedure. Although islet transplantation avoids the complications associated with whole pancreas transplantations, its clinical applications maintain significant drawbacks, including long-term immunosuppression, a lack of compatible donors, and blood-mediated inflammatory responses. Biomaterial-assisted islet transplantation is an emerging technology that embeds desired cells into biomaterials, which are then directly transplanted into the patient, overcoming the aforementioned challenges. Among various biomaterials, hydrogels are the preferred biomaterial of choice in these transplants due to their ECM-like structure and tunable properties. This review aims to present a comprehensive overview of hydrogel-based biomaterials that are engineered for encapsulation of insulin-secreting cells, focusing on new hydrogel design and modification strategies to improve beta-cell viability, decrease inflammatory responses, and enhance insulin secretion. We will discuss the current status of clinical studies using therapeutic bioengineering hydrogels in insulin release and prospective approaches.
引用
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页数:24
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